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运动介导的改善与糖尿病前期相关的痛性周围神经病的小鼠模型。

Exercise-mediated improvements in painful neuropathy associated with prediabetes in mice.

机构信息

Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.

出版信息

Pain. 2013 Dec;154(12):2658-2667. doi: 10.1016/j.pain.2013.07.052. Epub 2013 Aug 6.

Abstract

Recent research suggests that exercise can be effective in reducing pain in animals and humans with neuropathic pain. To investigate mechanisms in which exercise may improve hyperalgesia associated with prediabetes, C57Bl/6 mice were fed either standard chow or a high-fat diet for 12 weeks and were provided access to running wheels (exercised) or without access (sedentary). The high-fat diet induced a number of prediabetic symptoms, including increased weight, blood glucose, and insulin levels. Exercise reduced but did not restore these metabolic abnormalities to normal levels. In addition, mice fed a high-fat diet developed significant cutaneous and visceral hyperalgesia, similar to mice that develop neuropathy associated with diabetes. Finally, a high-fat diet significantly modulated neurotrophin protein expression in peripheral tissues and altered the composition of epidermal innervation. Over time, mice that exercised normalized with regards to their behavioral hypersensitivity, neurotrophin levels, and epidermal innervation. These results confirm that elevated hypersensitivity and associated neuropathic changes can be induced by a high-fat diet and exercise may alleviate these neuropathic symptoms. These findings suggest that exercise intervention could significantly improve aspects of neuropathy and pain associated with obesity and diabetes. Additionally, this work could potentially help clinicians determine those patients who will develop painful versus insensate neuropathy using intraepidermal nerve fiber quantification.

摘要

最近的研究表明,运动对于减轻动物和人类神经性疼痛具有一定的效果。为了研究运动改善糖尿病前期相关痛觉过敏的机制,将 C57Bl/6 小鼠分为两组,一组喂食标准食物(正常饮食),另一组喂食高脂肪食物(高脂肪饮食)12 周,同时提供跑步轮(运动组)或不提供跑步轮(久坐组)。高脂肪饮食导致了多种糖尿病前期症状,包括体重增加、血糖和胰岛素水平升高。运动虽降低了这些代谢异常,但未能使其恢复至正常水平。此外,高脂肪饮食组的小鼠出现了明显的皮肤和内脏痛觉过敏,与发生与糖尿病相关的神经病变的小鼠类似。最后,高脂肪饮食显著改变了周围组织的神经营养因子蛋白表达,并改变了表皮神经支配的组成。随着时间的推移,运动组的小鼠在行为过敏、神经营养因子水平和表皮神经支配方面逐渐恢复正常。这些结果证实,高脂肪饮食可引起敏感性升高和相关的神经病变变化,而运动可能缓解这些神经病理性症状。这些发现表明,运动干预可能会显著改善肥胖和糖尿病相关的神经病变和疼痛的多个方面。此外,这项工作还有助于临床医生通过表皮内神经纤维定量来确定哪些患者会发展为有痛性或无痛性神经病变。

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